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Differential
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abducens nerve paralysis
acetazolamide
acromegaly
adverse drug reaction
alcohol
Alexanders disease
Alexanders disease, adult onset
algorithm
alternating hemiplegia
alternating hemiplegia of childhood
amaurosis fugax
aminoacidopathies
aminoacidurias
amyloid angiopathy, cerebral
anemia
aneurysm
angiography, cerebral, beaded vessels
angiography, cerebral
angiography, cerebral, negative
angiography, vertebral artery
anorexia
anti IgLON5
antibodies to voltage-gated calcium channels
anxiety
aphasia
apnea
areflexia
arteritides
arteritis, temporal
arthralgia
astrogliopathy
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, truncal
ataxic gait
ATP1A3 gene
autoantibodies
autoimmune disease
autonomic dysfunction
behavioral disorder
blindness
brain biopsy
brainstem, infarction of
brainstem, lesion of
bulbar palsy
calcium antagonist
calcium channel dysfunction
carbamazepine
CAT scan
CAT scan, abnormal
CAT scan, angiography
cataracts
central core disease
central retinal artery occlusion
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar degeneration
cerebellar lesion
cerebellar vermis
cerebral infarction
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, young adult
channelopathy
Charcot-Marie-Tooth
chemotherapy, CNS treatment and complications with
children
chills
chloride channel dysfunction
chorea
chromosomal abnormality
chromosome 19
ciguatera poisoning
Clinical Pathologic Conference(C.P.C.)
cognition
collagen vascular disease
coma
coma, episodic
complications
confusion
conversion reaction
cornea, abnormal
cough
deafness
deafness, unilateral
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
delirium
dementia
dementia, rapidly progressive
dentate nuclei, lesion of
depression
developmental retardation
diabetes insipidus
diagnostic criteria
differential diagnosis
digital subtraction angiography
diplopia
diurnal variation
down-beat nystagmus
down-beat nystagmus, primary position of gaze
drug induced neurologic disorders
dysarthria
dysphagia
dystonia
dystonia, psychogenic
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
encephalitis
encephalitis, autoimmune
encephalopathy
encephalopathy, acute
episodic disorders
episodic neurologic deficits
episodic unconsciousness
epistaxis
exercise
exercise intolerance
eye movement, disorders of
face, numbness of
facial nerve palsy
facial weakness
faciobrachial dystonic seizure
failure to thrive
falling
familial
familial hemiplegic migraine
familial periodic ataxia
fasciculation
fatigue
fever
fine motor function, impaired
Friedreich's ataxia
fundus, abnormality of
gait disorder
gene
gene mutation
genetic neurologic disorders
genetic testing
GFAP gene
glaucoma
globus pallidus, lesion of, bilateral
Guillain Barre syndrome
gynecomastia
hallucination
hallucination, visual
head turning
head turning, neurologic complications with
headache
headache, bifrontal
headache, elderly
headache, occipital
headache, recurrent
headache, severe
hearing loss
hemianopia
hemianopia, homonymous
hemimyoclonic jerks
hemiparesis
hemiplegia
hepatomegaly
hoarseness
hypercalcemia
hyperparathyroidism
hyperreflexia
hypersomnia
hypertension
hyperthyroidism
hypokalemia
hypokalemic periodic paralysis
hyponatremia
hypophonia
hypotonia
iatrogenic neurologic disorders
imbalance
immunotherapy
inborn errors of metabolism
incoordination
infection
intellectual deficit
intracerebral hemorrhage
iritis
jaw claudication
lactic acidemia
lateropulsion
leg numbness
leg weakness, bilateral
lethargy
leucine rich glioma inactivated 1 antibodies
leukemia
leukodystrophy
leukoencephalopathy
limbic encephalitis
lysosomal storage disease
macrocephaly
malignant hyperpyrexia
maple syrup urine disease
mastoiditis
memory, defect of recent
memory, impairment of
meningeal enhancement
meningitis
meningitis, aseptic
meningitis, carcinomatous
meningitis, elderly
mental status, abnormal
metabolic disorder, primary
methotrexate
microcephaly
microhemorrhage, intracerebral
migraine
migraine, hemiplegic
misdiagnosis
molecular genetics
mononeuropathy
mononeuropathy multiplex
monoparesis
mortality
motor dysfunction
motor neuron disease
motor neuron disease, misdiagnosis
movement disorder
movement disorder, hyperkinetic
movement disorder, psychogenic
MRI
MRI, abnormal
MRI, angiography
MRI, diffusion weighted
MRI, negative
MRI, spine
multimodal neuroimaging
multiple sclerosis
multiple sclerosis, pain in
multiple sclerosis, paroxysmal symptoms in
muscle biopsy
muscle cramp
muscle pain
muscle weakness
muscle weakness, proximal
myasthenic syndrome
myoclonic jerks
myoclonus
myokymia
myotonia
myotonia congenita
nasal septum, perforation of
nausea and vomiting
negative
neuroendocrinology
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neurologic examination, focal
neurologic signs
neurologic symptoms
neurologic symptoms, unexplained
neurologic testing
neuromyotonia
neuroophthalmology
neuropathy
neuropathy, hereditary peripheral
neuropathy, peripheral
neuropathy, vasculitic, systemic
neurotoxic
neurotoxicity, acute
night sweats
nystagmus
nystagmus, gaze-paretic
nystagmus, hereditary
nystagmus, intermittent
nystagmus, monocular
nystagmus, periodic
nystagmus, vertical
old age, neurology of
ophthalmoplegia
optic ataxia
optic atrophy
optic neuritis
optic neuropathy, ischemic
oscillopsia
otitis, neurologic complications with
pain
pain, abdominal
pain, leg
pain, testicular
palatal myoclonus
palinopsia
papilledema
paralysis
paralysis, acute areflexic
paramyotonia congenita
paraparesis
paresthesias
Parkinson disease, dystonia with
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
paroxysmal tonic upgaze
pathology
periarteritis nodosa
periodic paralysis
periodic paralysis, thyrotoxic
peroxisomal disease
personality disorder
pleocytosis of cerebrospinal fluid
polyneuropathy
polyuria
posterior leukoencephalopathy syndrome
potassium
potassium channel antibodies
potassium channel dysfunction
precipitating factors
pregnancy, neurologic complications in
primary episodic ataxia
prognosis
progressive neurologic disorder
psychiatric disorder
psychiatric problems in neurologic disorders
psychosis
psychosis, acute
ptosis
pulmonary infiltrates
pupil, abnormality in neurologic disorders
pupil, tonic
quadriplegia
quadriplegia, transient
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
rash
recurrent
REM sleep behavior disorder
retinal artery occlusion
retinopathy
reversible cerebral vasoconstrictive syndromes
review article
rheumatoid arthritis
rheumatoid arthritis factor(R.A.factor)
rhinorrhea
scleritis
scotoma
sedimentation rate, elevated
seizure
seizure, differential diagnosis of
seizure, focal
sensorineural hearing loss
sinusitis
skin, lesions in neurologic disorders
sleep pathology and physiology
sodium channel dysfunction
sore throat
spinal cord, compression of
spinal stenosis
spinal stenosis, cervical canal
spinocerebellar ataxia
spinocerebellar ataxia type 6
status epilepticus
steroid therapy, CNS treatment and complications with
stress, emotional
strokelike episodes
subarachnoid hemorrhage, cerebral convexity
symmetric brain lesions
syncope
tachycardia
tandem gait, ataxic
temporal lobe, lesion, bilateral
testicular biopsy
third nerve palsy
thirst
thyrotoxicosis
tinnitus
tonic spasms
toxic encephalopathy
transient ischemic attack
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, psychogenic
trigeminal neuralgia
trigeminal neuropathy
trigeminal neuropathy, sensory
trinucleotide repeats
unconsciousness
unconsciousness, episodic
unconsciousness, transient
upgaze
upgaze, sustained
urea-cycle enzymopathies
uremia
vaccination, neurologic complications with
vasculopathy
vasospasm, cerebral
vertebral artery
vertebral artery disease
vertebral artery occlusion
vertebral artery stenosis
vertebral-basilar insufficiency
vertigo
vertigo, episodic
Virchow-Robin spaces, dilated
vision, blurred
visual field defect
visual loss
vitamin E deficiency
vocalizations
walking, difficulty with
weakness
weakness, acute
weakness, episodic
weakness, generalized
weight loss
white matter disease
wide based gait
Showing articles 0 to 50 of 1608 Next >>

Clinicopathologic Conference, Anti-IgLON5 IgG-Associated Neurologic Disorder
NEJM 386:173-180, Case 1-2022, 2022

A 55-Year-Old Woman with Recurrent Episodes of Aphasia and Vision Changes
Neurol 98:330-335, Jeanneret, V.,et al, 2022

The Phenotypic Continuum of ATP1A3-Related Disorders
Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022

Paraoxysmal Tonic Upgaze in Children, Three Case Reports and a Review of the Literature
Pediatr Emer Care 35:e67-e69, Kartal,A., 2019

When MRI is a Clue in Episodic Ataxia
Neurol 93:e2074-e2075, Dhawan, S.R.,et al, 2019

Strokelike Episodes in a Patient with Chronic Gait Abnormalities
JAMA Neurol 76:621-622, Santoro, J.D. & Chitnis, T., 2019

A 72-year-old Man with Rapid Cognitive Decline and Unilateral Muscle Jerks
Neurol 82:e194-e197, Duncan, M.,et al, 2014

Multimodal Imaging of Reversible Cerebral Vasoconstriction Syndrome: A Series of 6 Cases
AJNR 33:1403-1410, Marder, C.P.,et al, 2012

Clincopathologic Conference,Graves Disease with Thyrotoxic Periodic Paralysis
NEJM 366:553-560, Case 4-2012, 2012

GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
Neurol 77:1287-1294, Prust, M.,et al, 2011

Age and High-Dose Methotrexate are Associated to Clinical Acute Encephalopathy in FRALLE 93 Trial for Acute Lymphoblastic Leukemia in Children
Leukemia 21:238-247, Dufourg, M.N.,et al, 2007

Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
Brain 130:2484-2493, Jen, J.C.,et al, 2007

Clinical Spectrum of Episodic Ataxia Type 2
Neurol 62:17-22, Jen,J.,et al, 2004

Rotational Vertebral Artery Occlusion Syndrome with Vertigo Due to "Labyrinthine Excitation"
Neurol 54:1376-1379, Strupp,M.,et al, 2000

Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
JNNP 69: 5-12, Gray,R.G.F. et al, 2000

Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
JNNP 65:427-431, Hanna,M.G.,et al, 1998

Neurological Channelopathies, Dysfunctional Ion Channels May Cause Many Neurological Diseases
BMJ 316:1104-1105, Rose,M.R., 1998

Slater Revisited:6 Year Follow Up Study of Pts with Medically Unexplained Motor Symptoms
BMJ 316:582-586, 5641998., Crimlisk,H.L.,et al, 1998

Spinocerebellar Ataxia Type 6, Frequency of the Mutation & Genotype-Phenotype Correl
NEurol 49:1247-1251, Geschwind,D.H.,et al, 1997

Calcium Channels in Neurological Disease
Ann Neurol 42:275-282, Greenberg,D.A., 1997

Familial episodic Ataxia:Clinical Heterogeneity in Four Families Linked to Chromosome 19p
Ann Neurol 41:8-16, 41997., Baloh,R.W.,et al, 1997

The Inherited Ataxias and the New Genetics
JNNP 61:327-332, Hammans,S.R., 1996

A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
Ann Neurol 37:289-293, 2851995., Vahedi,K.,et al, 1995

Acute Quadriplegia in Acromegaly
Ann Int Med 117:94-95, Tanigawa,K.,et al, 1992

Neurologic Manifestations of Giant Cell Arteritis
Am J Med 89:67-72, Reich,K.A.,et al, 1990

Paroxysmal Cerebellar Ataxia
Aust NZ J Med 19:113-117, Feeney,G.F.&Boyle,R.S., 1989

Magnetic Resonance Imaging in Familial Paroxysmal Ataxia
Arch Neurol 45:547-549, Vighetto,A.,et al, 1988

Acetazolamide-Responsive Episodic Ataxia Syndrome
Neurol 33:1212-1214, Zasorin,N.L.,et al, 1983

Focal Neurologic symptoms in hypercalcemia
Neurol 30:200-201, Longo,D.L.,et al, 1980

Paroxysmal Symptoms as the First Manifestations of Multiple Sclerosis
JNNP 43:296-304, Twomey,J.A.,et al, 1980

Familial Periodic Ataxia
Arch Neurol 36:568-569, Donat,J.R.,et al, 1979

Hereditary Paroxysmal Ataxia:Response to Acetazolamide
Neurol 28:1259-1264, Griggs,R.C.,et al, 1978

Central Nervous System Manifestations of Periarteritis Nodosa
Neurol 15:114, Ford,R.G.,et al, 1965

A 60-Year-Old Man with Weakness and Gait Dysfunction
JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025

A 67 YEar-Old Woman with Progressive Headache, Visual Hallucinations, and Seizures
Neurol 104:e213496, Gheihman,G.,et al, 2025

A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
Neurol 104:e213593, Pence, K.L. &Clark, R.A., 2025

A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
Neurol 104:e213713, Rawat,R.,et al, 2025

A 59-Year-Old Man with Progressive Dysarthria and Gait Instability
Neurol 104:e213729, Shen,D.,et al, 2025

Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
Cureus doi:10.7759/CUREUS.32182, Sweedan,Y.G.,et al, 2025

A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025

Stroke-Like Migraine Attacks After Radiation Therapy Syndrome
Neurol 104:e210203, Lubotzky,A.,t al, 2025

A 68-YEar-Old Man with Progressive Numbness, Vertigo, and Cognitive Decline
Neurol 104:e213437, Regan,S.M. & Davalos,L.F., 2025

Methamphetamine-Induced Basal Ganglia Toxicity Presenting as Parkinsonism
Neurol 104:e213365, Yi,M.Y.,et al, 2025

Epidural Steroids for Cervical and Lumbar Radicular Pain and Spinal Stenosis Systematic Review Summary
Neurol 104:e213361, Armon,C.,et al, 2025

Juvenile-Onset Dopa-Responsive Dystonia-Until It Isnt
Neurol 104:e213436, Paredes,N.C.,et al, 2025

Vitamin B12 Deficiency:NICE Guideline Summary
BMJ 385:q1019, q1262, Sands,T.,et al, 2024

Expanding Clinical Spectrum an Anti-GQ1b Antibody Syndrome, A Review
JAMA Neurol 81:762-770, Lee,S-U.,et al, 2024

Hyperventilation-Induced Alternating Hemiplegia with Concomitant Hemispheric EEG Slowing in a 7-Year-Old Girl with Headache
Neurol 103:e209759, Proietti,J.,et al, 2024

Vestibular Drop Attacks Diagnosed with Valuable Insights from CCTV
Lancet 404:787-788, Joffily,L.,et al, 2024



Showing articles 0 to 50 of 1608 Next >>